Canonical Allele Identifier: CA1017976908
Gene: SLC2A10 HGNC NCBI

Linked Data

dbSNP Id: rs1979855248

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46725520del , CM000682.2:g.46725520del GRCh38
NC_000020.10:g.45354159del , CM000682.1:g.45354159del GRCh37
NC_000020.9:g.44787566del NCBI36
NG_016284.1:g.20881del

Transcript Alleles

HGVS Amino-acid Change
ENST00000359271.4:c.484del MANE Select ENSP00000352216.2:p.Trp162GlyfsTer?
ENST00000359271.3:c.484del ENSP00000352216.2:p.Trp162GlyfsTer?
NM_030777.3:c.484del NP_110404.1:p.Trp162GlyfsTer?
XM_011529060.1:c.547del XP_011527362.1:p.Trp183GlyfsTer?
XM_011529061.1:c.493del XP_011527363.1:p.Trp165GlyfsTer?
XM_011529062.1:c.547del XP_011527364.1:p.Trp183GlyfsTer?
XM_011529063.1:c.547del XP_011527365.1:p.Trp183GlyfsTer?
XM_011529064.1:c.547del XP_011527366.1:p.Trp183GlyfsTer?
XM_011529065.1:c.547del XP_011527367.1:p.Trp183GlyfsTer?
XR_936641.1:n.683del
XM_011529060.2:c.547del XP_011527362.1:p.Trp183GlyfsTer?
XM_011529061.2:c.493del XP_011527363.1:p.Trp165GlyfsTer?
XM_011529062.2:c.547del XP_011527364.1:p.Trp183GlyfsTer?
XM_011529063.2:c.547del XP_011527365.1:p.Trp183GlyfsTer?
XM_011529064.2:c.547del XP_011527366.1:p.Trp183GlyfsTer?
XM_011529065.2:c.547del XP_011527367.1:p.Trp183GlyfsTer?
XM_017028087.2:c.484del XP_016883576.1:p.Trp162GlyfsTer?
XR_936641.2:n.670del
NM_030777.4:c.484del MANE Select NP_110404.1:p.Trp162GlyfsTer?